HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-chloro-3-(piperidin-4-yl)-1H-indole → HCID 131724872, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-chloro-3-(piperidin-4-yl)-1H-indole | HCID 12072036 | — |
| Reactant | HCID 22484004 | HCID 22484004 | — |
| Product | HCID 131724872 | HCID 131724872 | — |
Reaction Steps
from 7-chloro-3-(piperidin-4-yl)-1H-indole and 3-bromo-1-(3,4-dihydro-1H-isoquinolin-2-yl)propan-1-one. 1H NMR (DMSO-d6): 2.05-2.25 (m, 4H); 2.80 (t, 0.8H); 2.95 (t, 1.2H); 3.00-3.20 (m, 5H); 3.30-3.45 (m, 2H); 3.55-3.65 (m, 2H); 3.65-3.75 (m, 2H); 4.65 (s, 1.2H); 4.75 (s, 0.8H); 7.00 (t, 1H); 7.15-7.25 (m, 6H); 7.70 (d, 1H); 10.70 (broad s, 1H); 11.30 (s, 1H). MS m/z: 422 (MH+), 247.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07276508B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-65a4be962e2744f4bedcbd282f463863 |
| Source note | uspto-grants-2007_10 |